Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g27390 | A05 | 31665495 | G | A | missense_variant | MODERATE | c.2926C>T|p.Leu976Phe |
S15 S3 |
2 | BAA05g27390 | A05 | 31665788 | C | T | missense_variant | MODERATE | c.2747G>A|p.Gly916Glu |
S251 |
3 | BAA05g27390 | A05 | 31668597 | C | T | missense_variant | MODERATE | c.2126G>A|p.Arg709Lys |
S87 |
4 | BAA05g27390 | A05 | 31668849 | G | A | missense_variant | MODERATE | c.1874C>T|p.Ala625Val |
S236 |
5 | BAA05g27390 | A05 | 31669177 | G | A | missense_variant | MODERATE | c.1546C>T|p.His516Tyr |
S267 |
6 | BAA05g27390 | A05 | 31669837 | G | A | splice_region_variant&intron_variant | LOW | c.1027-3C>T| |
S275 |
7 | BAA05g27390 | A05 | 31671546 | C | T | upstream_gene_variant | MODIFIER | c.-172G>A| |
S10 S176 |
8 | BAA05g27390 | A05 | 31671604 | G | A | upstream_gene_variant | MODIFIER | c.-230C>T| |
S132 S137 |
9 | BAA05g27390 | A05 | 31671654 | G | A | upstream_gene_variant | MODIFIER | c.-280C>T| |
S163 |
10 | BAA05g27390 | A05 | 31671989 | C | T | upstream_gene_variant | MODIFIER | c.-615G>A| |
S105 S106 |